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Human embryonic stem-cell derivatives for full reconstruction of the pluristratified epidermis: a preclinical study
被引:167
作者:
Guenou, Hind
[1
]
Nissan, Xavier
[1
]
Larcher, Fernando
[2
]
Feteira, Jessica
[1
]
Lemaitre, Gilles
[1
]
Saidani, Manoubia
[1
]
Del Rio, Marcelo
[2
]
Barrault, Christine C.
[3
]
Bernard, Francois-Xavier
[3
]
Peschanski, Marc
[1
]
Baldeschi, Christine
[1
]
Waksman, Gilles
[1
]
机构:
[1] INSERM, I STEM, Inst Stem Cell Therapy & Explorat Monogen Dis, AFM,UEVE U 861, F-91030 Evry, France
[2] CIEMAT CIBER ER, Epithelial Biomed Div, Madrid, Spain
[3] BIOalternat SAS, Gencay, France
来源:
关键词:
GENE-EXPRESSION;
RETINOIC ACID;
SKIN;
DIFFERENTIATION;
KERATINOCYTES;
LINES;
REGENERATION;
MECHANISMS;
BANKING;
BURNS;
D O I:
10.1016/S0140-6736(09)61496-3
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background Cell therapy for large burns is dependent upon autologous epidermis reconstructed in vitro. However, the effectiveness of current procedures is limited by the delay needed to culture the patient's own keratinocytes. To assess whether the keratinocyte progeny of human embryonic stem cells (hESCs) could be used to form a temporary skin substitute for use in patients awaiting autologous grafts, we investigated the cells' capability of constructing a pluristratified epidermis. Methods hESCs from lines H9 and SA01 were seeded at least in triplicate on fibroblast feeder cells for 40 days in a medium supplemented with bone morphogenetic protein 4 and ascorbic acid. Molecular characterisation of cell differentiation was done throughout the process by quantitative PCR, fluorescence-activated cell sorting, and immunocytochemical techniques. Keratinocyte molecular differentiation and functional capacity to construct a human epidermis were assessed in vitro and in vivo. Findings From hESCs, we generated a homogeneous population of cells that showed phenotypic characteristics of basal keratinocytes. Expression levels of genes encoding keratin 14, keratin 5, integrin alpha 6, integrin beta 4, Collagen VII, and laminin 5 in these cells were similar to those in basal keratinocytes. After seeding on an artificial matrix, keratinocytes derived from hESCs (K-hESCs) formed a pluristratified epidermis. Keratin-14 immunostaining was seen in the basal compartment, with keratin 10 present in layers overlying the basal layer. Involucrin and filaggrin, late markers of epidermal differentiation, were detected in the uppermost layers only. 12 weeks after grafting onto five immunodeficient mice, epidermis derived from K-hESCs had a structure consistent with that of mature human skin. Human involucrin was appropriately located in spinous and granular layers and few Ki67-positive cells were detected in the basal layer. Interpretation hESCs can be differentiated into basal keratinocytes that are fully functional-ie, able to construct a pluristratified epidermis. This resource could be developed to provide temporary skin substitutes for patients awaiting autologous grafts.
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页码:1745 / 1753
页数:9
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